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Identification of TMPRSS3 as a Significant Contributor to Autosomal Recessive Hearing Loss in the Chinese Population

Hereditary hearing loss is characterized by a high degree of genetic heterogeneity. Mutations in the TMPRSS3 (transmembrane protease, serine 3) gene cause prelingual (DFNB10) or postlingual (DFNB8) deafness. In our previous study, three pathogenic mutations in TMPRSS3 were identified in one Chinese...

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Detalhes bibliográficos
Publicado no:Neural Plast
Main Authors: Gao, Xue, Huang, Sha-Sha, Yuan, Yong-Yi, Xu, Jin-Cao, Gu, Ping, Bai, Dan, Kang, Dong-Yang, Han, Ming-Yu, Wang, Guo-Jian, Zhang, Mei-Guang, Li, Jia, Dai, Pu
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi 2017
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5485344/
https://ncbi.nlm.nih.gov/pubmed/28695016
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2017/3192090
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